Canonical Allele Identifier: CA412982376
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535106A>G (hg19) chrX:g.38675852A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675852A>G , CM000685.2:g.38675852A>G GRCh38
NC_000023.10:g.38535106A>G , CM000685.1:g.38535106A>G GRCh37
NC_000023.9:g.38420050A>G NCBI36
NG_009160.1:g.119376A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.589A>G MANE Select ENSP00000367743.2:p.Asn197Asp
ENST00000286824.6:c.640A>G ENSP00000286824.6:p.Asn214Asp
ENST00000378482.6:c.589A>G ENSP00000367743.2:p.Asn197Asp
ENST00000419600.3:n.533A>G
ENST00000465127.1:c.679A>G ENSP00000417050.1:p.Asn227Asp
ENST00000471410.5:c.*615A>G ENSP00000419290.1:n.*615A>G
ENST00000475216.5:c.*582A>G ENSP00000418586.1:n.*582A>G
NM_004615.3:c.589A>G NP_004606.2:p.Asn197Asp
NM_004615.4:c.589A>G MANE Select NP_004606.2:p.Asn197Asp
Search 100 bp 5'
Search 100 bp 3'